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HRID 368903作成日:2026年10月26日

Sodium Chloride → (1S)-[(2R)-(2,4-difluorophenyl)-2-oxiranyl]ethanol

https://huagongshe.com/reaction/368903

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物tert-Butyl hydroperoxideHCID 6410—
反応物Sodium HydroxideHCID 14798—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Diethyl tartrateHCID 6993580—
反応物(2S)-3-(2,4-Difluorophenyl)-3-buten-2-olHCID 15130435—
触媒Titanium isopropoxideHCID 11026—
溶媒DichloromethaneHCID 6344—
生成物(1S)-[(2R)-(2,4-difluorophenyl)-2-oxiranyl]ethanolHCID 10631861—

反応条件

温度-5 °C

反応手順

To a solution of diethyl L(+)-tartrate (32.2 ml, 0.188 mole) in dry CH2Cl2 (5 L) is added activated 3A° molecular sieve powder (120 g) and cooled the mixture to -5 ° C. Added a solution of titanium (IV) isopropoxide (120 ml, 0.4 mole) followed by t-butyl hydroperoxide (312 ml of 5-6M solution in decane) and continue to stir at -5 ° C. for 25 minutes. To this mixture, a solution of crude 6a in CH2Cl2 (400 ml) is added and stirred for 12 hours at 5° C. Cooled the reaction mixture to -40° C., added 280 ml of 30% aq. NaOH solution saturated with NaCl and the mixture is allowed to warm to 10° C. Added 250 g of MgSO4, 80 g of celite and continued to stir at 10° C. for 30 minutes. The mixture is suction-filtered over celite. To the filtrate toluene (4 L) and 3 L of ether are added and insoluble material removed by filtration. The filtrate is evaporated under reduced pressure to give the crude 7a as oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06133485
出典データセットuspto-grants-2000_10
ORD IDord-d643c81a52ac4b678f971e3e61537779
出典メモuspto-grants-2000_10